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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1947 1
1949 1
1950 4
1952 1
1956 1
1957 1
1958 1
1960 2
1967 1
1968 1
1969 1
1971 1
1972 1
1975 3
1976 2
1977 3
1978 4
1979 4
1980 3
1981 1
1982 2
1983 5
1984 3
1985 2
1986 3
1987 3
1988 2
1989 6
1990 7
1991 5
1992 6
1993 7
1994 5
1995 5
1996 9
1997 6
1998 13
1999 10
2000 7
2001 9
2002 6
2003 11
2004 15
2005 12
2006 18
2007 13
2008 15
2009 11
2010 10
2011 11
2012 17
2013 20
2014 19
2015 16
2016 13
2017 13
2018 18
2019 18
2020 18
2021 15
2022 13
2023 17

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Article type

Publication date

Search Results

424 results

Results by year

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Page 1
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia.
Van de Vondel L, De Winter J, Beijer D, Coarelli G, Wayand M, Palvadeau R, Pauly MG, Klein K, Rautenberg M, Guillot-Noël L, Deconinck T, Vural A, Ertan S, Dogu O, Uysal H, Brankovic V, Herzog R, Brice A, Durr A, Klebe S, Stock F, Bischoff AT, Rattay TW, Sobrido MJ, De Michele G, De Jonghe P, Klopstock T, Lohmann K, Zanni G, Santorelli FM, Timmerman V, Haack TB, Züchner S; PREPARE Consortium; Schüle R, Stevanin G, Synofzik M, Basak AN, Baets J. Van de Vondel L, et al. Among authors: de michele g. Mov Disord. 2022 Jun;37(6):1175-1186. doi: 10.1002/mds.28959. Epub 2022 Feb 12. Mov Disord. 2022. PMID: 35150594 Free PMC article.
NGS in Hereditary Ataxia: When Rare Becomes Frequent.
Galatolo D, De Michele G, Silvestri G, Leuzzi V, Casali C, Musumeci O, Antenora A, Astrea G, Barghigiani M, Battini R, Battisti C, Caputi C, Cioffi E, De Michele G, Dotti MT, Fico T, Fiorillo C, Galosi S, Lieto M, Malandrini A, Melone MAB, Mignarri A, Natale G, Pegoraro E, Petrucci A, Ricca I, Riso V, Rossi S, Rubegni A, Scarlatti A, Tinelli F, Trovato R, Tedeschi G, Tessa A, Filla A, Santorelli FM. Galatolo D, et al. Among authors: de michele g. Int J Mol Sci. 2021 Aug 6;22(16):8490. doi: 10.3390/ijms22168490. Int J Mol Sci. 2021. PMID: 34445196 Free PMC article.
Antiphospholipid-related chorea.
Peluso S, Antenora A, De Rosa A, Roca A, Maddaluno G, Brescia Morra V, De Michele G. Peluso S, et al. Among authors: de michele g. Front Neurol. 2012 Oct 22;3:150. doi: 10.3389/fneur.2012.00150. eCollection 2012. Front Neurol. 2012. PMID: 23097646 Free PMC article.
Spinocerebellar ataxia type 48: last but not least.
De Michele G, Galatolo D, Barghigiani M, Dello Iacovo D, Trovato R, Tessa A, Salvatore E, Filla A, De Michele G, Santorelli FM. De Michele G, et al. Neurol Sci. 2020 Sep;41(9):2423-2432. doi: 10.1007/s10072-020-04408-3. Epub 2020 Apr 27. Neurol Sci. 2020. PMID: 32342324 Review.
Of cognition and cerebellum in SCA48.
De Michele G, Salvatore E, Cocozza S, Filla A, Santorelli FM. De Michele G, et al. Neurogenetics. 2020 Apr;21(2):145-146. doi: 10.1007/s10048-020-00603-8. Epub 2020 Feb 3. Neurogenetics. 2020. PMID: 32009217 No abstract available.
Degenerative and acquired sporadic adult onset ataxia.
Lieto M, Roca A, Santorelli FM, Fico T, De Michele G, Bellofatto M, Saccà F, De Michele G, Filla A. Lieto M, et al. Among authors: de michele g. Neurol Sci. 2019 Jul;40(7):1335-1342. doi: 10.1007/s10072-019-03856-w. Epub 2019 Mar 29. Neurol Sci. 2019. PMID: 30927137 Review.
STUB1-Related Ataxias: A Challenging Diagnosis.
Cocozza S, Santorelli FM, De Michele G. Cocozza S, et al. Among authors: de michele g. Mov Disord Clin Pract. 2020 Jul 19;7(6):733-734. doi: 10.1002/mdc3.12992. eCollection 2020 Aug. Mov Disord Clin Pract. 2020. PMID: 32775533 Free PMC article. No abstract available.
Overview of autosomal recessive ataxias.
Filla A, De Michele G. Filla A, et al. Among authors: de michele g. Handb Clin Neurol. 2012;103:265-74. doi: 10.1016/B978-0-444-51892-7.00016-4. Handb Clin Neurol. 2012. PMID: 21827894 Review. No abstract available.
The Multiple Faces of Spinocerebellar Ataxia type 2.
Antenora A, Rinaldi C, Roca A, Pane C, Lieto M, Saccà F, Peluso S, De Michele G, Filla A. Antenora A, et al. Among authors: de michele g. Ann Clin Transl Neurol. 2017 Aug 10;4(9):687-695. doi: 10.1002/acn3.437. eCollection 2017 Sep. Ann Clin Transl Neurol. 2017. PMID: 28904990 Free PMC article. Review.
424 results